Pages that link to "Q35113387"
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The following pages link to Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction (Q35113387):
Displaying 50 items.
- Mitochondrial diabetes in children: seek and you will find it (Q21090926) (← links)
- Mitochondrial tRNA mutations and disease (Q26828352) (← links)
- The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity (Q28392028) (← links)
- Analysis of mitochondrial DNA variations in Indian patients with congenital cataract (Q28396290) (← links)
- Mitochondrial disease in autism spectrum disorder patients: a cohort analysis (Q28474112) (← links)
- Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management (Q30459704) (← links)
- Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variants (Q33300347) (← links)
- A reduced number of mtSNPs saturates mitochondrial DNA haplotype diversity of worldwide population groups (Q33573477) (← links)
- Long survival in patients with leigh syndrome and the m.10191T>C mutation in MT-ND3 : a case report and review of the literature (Q33671457) (← links)
- Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases (Q33942825) (← links)
- The optic nerve: a "mito-window" on mitochondrial neurodegeneration (Q34298350) (← links)
- A mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives (Q34325643) (← links)
- Role of mtDNA haplogroups in the prevalence of osteoarthritis in different geographic populations: a meta-analysis (Q34395045) (← links)
- Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy. (Q34514611) (← links)
- Characterization of macular thickness changes in Leber's hereditary optic neuropathy by optical coherence tomography (Q34538766) (← links)
- A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. (Q34551734) (← links)
- An Incompatibility between a mitochondrial tRNA and its nuclear-encoded tRNA synthetase compromises development and fitness in Drosophila (Q34574918) (← links)
- Mito-nuclear co-evolution: the positive and negative sides of functional ancient mutations (Q34763439) (← links)
- An MRPS12 mutation modifies aminoglycoside sensitivity caused by 12S rRNA mutations (Q34955098) (← links)
- Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy (Q35076141) (← links)
- Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice (Q35510598) (← links)
- Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy. (Q35593390) (← links)
- Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy? (Q35636297) (← links)
- Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains (Q38636513) (← links)
- Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach (Q35988151) (← links)
- Dominance in mitochondrial disorders. (Q36114785) (← links)
- Neuron-specific enolase is elevated in asymptomatic carriers of Leber's hereditary optic neuropathy (Q36257889) (← links)
- Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways (Q36485172) (← links)
- The role of mitochondria in inherited neurodegenerative diseases (Q36521932) (← links)
- Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation (Q36676493) (← links)
- Mitochondrial DNA variations in Madras motor neuron disease (Q36722312) (← links)
- Evidence for nuclear modifier gene in mitochondrial cardiomyopathy (Q37340280) (← links)
- Pathogenic mutations of nuclear genes associated with mitochondrial disorders (Q37412986) (← links)
- Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss (Q39412964) (← links)
- Characterization of retinal nerve fiber layer thickness changes associated with Leber's hereditary optic neuropathy by optical coherence tomography (Q41851186) (← links)
- Strain-specific nuclear genetic background differentially affects mitochondria-related phenotypes in Saccharomyces cerevisiae (Q42120152) (← links)
- IL-1β hampers glucose-stimulated insulin secretion in Cohen diabetic rat islets through mitochondrial cytochrome c oxidase inhibition by nitric oxide (Q42707401) (← links)
- Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON). (Q43826118) (← links)
- The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees (Q44086295) (← links)
- The G1888A variant in the mitochondrial 16S rRNA gene may be associated with Type 2 diabetes in Caucasian-Brazilian patients from southern Brazil (Q44556750) (← links)
- Analysis of the mitochondrial genome of cheetahs (Acinonyx jubatus) with neurodegenerative disease (Q45012312) (← links)
- Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes. (Q48639506) (← links)
- Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion. (Q46696039) (← links)
- Bioactivity and Gene Expression Profiles of hiPSC-generated Retinal Ganglion Cells in MT-ND4 Mutated Leber's Hereditary Optic Neuropathy. (Q47647290) (← links)
- A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations. (Q48056181) (← links)
- Novel mitochondrial mutation in the ND4 gene associated with Leigh syndrome (Q48403825) (← links)
- Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy (Q50000914) (← links)
- The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease (Q50994607) (← links)
- Mitochondrial DNA in tumors (Q51636764) (← links)
- Leber's hereditary optic neuropathy - Case report. (Q55068873) (← links)